Non-muscle Myosin-II Is Required for the Generation of a Constriction Site for Subsequent Abscission

被引:25
|
作者
Wang, Kangji [1 ]
Wloka, Carsten [1 ,2 ]
Bi, Erfei [1 ]
机构
[1] Univ Penn, Dept Cell & Dev Biol, Perelman Sch Med, Philadelphia, PA 19104 USA
[2] Univ Groningen, Groningen Biomol Sci & Biotechnol Inst, NL-9747 AE Groningen, Netherlands
关键词
ESCRT-III; BLEBBISTATIN INHIBITION; CYTOKINETIC ABSCISSION; DISTINCT ROLES; MIDBODY; DYNAMICS; MECHANISMS; MACHINERY; ISOFORMS; SPASTIN;
D O I
10.1016/j.isci.2019.02.010
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
It remains unknown when, where, and how the site of abscission is generated during cytokinesis. Here, we show that the sites of constriction, i.e., the sites of future abscission, are initially formed at the ends of the intercellular bridge during early midbody stage, and that these sites are associated with the non-muscle myosin-IIB (not myosin-IIA), actin filaments, and septin 9 until abscission. The ESCRT-III component CHMP4B localizes to the midbody and "spreads" to the site of abscission only during late midbody stage. Strikingly, inhibition of myosin-II motor activity by a low dose of Blebbistatin completely abolishes the formation of the constriction sites, resulting in the localization of all the above-mentioned components to the midbody region. These data strongly suggest that a secondary actomyosin ring provides the primary driving force for the thinning of the intercellular bridge to allow ESCRT-mediated membrane fission.
引用
收藏
页码:69 / +
页数:30
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